591-09-3

Basic information

• Product Name: nitro acetate
• Synonyms: nitro acetate
• CAS NO: 591-09-3
• Molecular Formula: C₂H₃NO₄
• Molecular Weight: 105.06
• Mol File: 591-09-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: bp70 22°
• Flash Point: 92.3°C
• Appearance: /
• Density: d415 1.24
• Vapor Pressure: 2.56mmHg at 25°C
• Refractive Index: 1.4264 (estimate)
• CAS DataBase Reference: nitro acetate(CAS DataBase Reference)
• NIST Chemistry Reference: nitro acetate(591-09-3)
• EPA Substance Registry System: nitro acetate(591-09-3)

Safety Data

• Hazardous Substances Data: 591-09-3(Hazardous Substances Data)

Usage

Uses

In nitrations, especially to introduce a single nitro group in an ortho position on an aromatic ring.

InChI:InChI=1/C2H3NO4/c1-2(4)7-3(5)6/h1H3

Upstream product

• 590-18-1 (Z)-2-Butene 

Downstream Products

• 700-58-3 2-Adamantanone 
• 87649-42-1 2-(nitromethylidene)adamantane 
• 133709-31-6 2-(α-Nitrobenzylidene)tricyclo<3.3.1.1^3,7>decane 
• 71756-89-3 2,4,6-trichloro-N-nitroaniline 
• 71757-13-6 2-Trifluoromethyl-4,6-dibromo-N-nitroaniline 
• 71756-96-2 2,6-dibromo-4-fluorophenylnitramine 
• 71756-95-1 2,6-dibromo-4-chloro-N-nitro-aniline 
• 71757-05-6 2,4-dibromo-6-chloro-N-nitro-aniline 
• 71757-00-1 2,4-dibromo-6-methyl-N-nitro-aniline 
• 20020-19-3 2,4,6-tribromo-N-nitro-aniline 
• 52917-31-4 2,6-dibromo-4-methyl-N-nitro-aniline 
• 78771-28-5 2-Methyl-3,5-dinitrothiophene 
• 42297-94-9 5-nitro-2-methylthiophene 
• 1021187-16-5 2-methyl-5-nitrothiophene S-oxide 

Relevant articles and documents

Cyclic diamine compounds and medicine containing the same

The present invention offers novel cyclic diamine compounds and a pharmaceutical composition containing the same. The present invention relates to a compound represented by the formula (I) or salt(s) or solvate(s) thereof. (In the formula, is an optionally substituted divalent residue of benzene, pyridine, cyclohexane or naphthalene or is a vinylene group where Ar is an optionally substituted aryl group;X is —NH—, oxygen atom or sulfur atom;Y is —NR1—, oxygen atom, sulfur atom, sulfoxide or sulfone;Z is a single bond or —NR2—;R1 is hydrogen atom, optionally substituted lower alkyl group, optionally substituted aryl group or optionally substituted silyl lower alkyl group;R2 is hydrogen atom, optionally substituted lower alkyl group, optionally substituted aryl group or optionally substituted silyl lower alkyl group;l is an integer of from 0 to 15;m is an integer of 2 or 3; andn is an integer of from 0 to 3). The compound of the present invention is useful as a pharmaceutical composition, particuarly as an inhibitor of acyl coenzyme A cholesterol acyltransferase (ACAT).

Linear-Reactor-IR.-Matrix and Microwave Spectroscopy of the System O3/NO2/(Z)-2-Butene

Investigation of the formation of complex reaction products in the gas-phase system O3/NO2/(Z)-2-butene by combination of linear reactors with IR. matrix and microwave Stark spectroscopy is reported.Besides the polyatomic products observed earlier in the gas-phase ozonolysis of (Z)-2-butene, the following products were identified: N2O5, HNO3, HNO4, CH3NO2, CH3ONO, CH3COONO2 and CH3COO2NO2 (peroxyacetyl nitrate PAN).Matrix IR spectra of N2O5, HNO3, CH3COONO, CH3COONO2 required for reference purposes are presented.It is shown that PAN-formation occurs already in the absence of light.A reaction scheme is proposed for explanation of the observed complex NOx-containing products, which assumes methyldioxirane as a central intermediate.Particular reaction steps of the scheme will be discussed, including thermochemical estimates of reaction enthalpies.